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Sr2+和Mg2+对磷脂酶A以及β-银环蛇毒素、响尾蛇毒素和太攀蛇毒素的突触前神经肌肉阻断作用的影响。

Effects of Sr2+ and Mg2+ on the phospholipase A and the presynaptic neuromuscular blocking actions of beta-bungarotoxin, crotoxin and taipoxin.

作者信息

Chang C C, Su M J, Lee J D, Eaker D

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Sep;299(2):155-61. doi: 10.1007/BF00498557.

Abstract

1.beta-Bungarotoxin, crotoxin and taipoxin, presynaptic neurotoxins of snake venom origin, have about the same phospholipid-splitting activities as a much less toxic cobra phospholipase A2 in the presence of Ca2+ and deoxycholate. 2. Sr2+ was a much less effective activator of the enzymes than is Ca2+, the activation by Sr2+ being only 3-6% for beta-bungarotoxin and crotoxin and 12% for taipoxin. 3. Sr2+ also inhibited the Ca2+ -activated enzymes by 80% in the cases of beta-bungarotoxin and crotoxin, but only 16% in the case of taipoxin. 4. Mg2" had no significant effect on beta-bungarotoxin or crotoxin, but activated taipoxin in the presence or absence of Ca2". 5. In Sr2+ -Tyrode lacking Ca2+ all three toxins exhibited the same immediate depression followed by facilitation in the rat and mouse diaphragms, but the final blocking activity was only 3-10% with beta-bungarotoxin and crotoxin and was 30% with taipoxin. 6. In Sr2+ -Tyrode, increasing in the rate of nerve stimulation had less accelerating effect on the development of neuromuscular block than in Ca2+ -Tyrode for any of the toxins. 7. Removal of Mg2+ from Sr2+ -Tyrode did not diminish the potency of taipoxin in blocking neuromuscular transmission, suggesting that enzyme activity at the outer surface of the axolemma does not contribute to the neuromuscular blocking action. 8. All of the results indicate that there are close correlations between the presynaptic activities of these toxins and their phospholipid-splitting activities in the cationic environment prevailing in the axoplasm. Apparently the final blocking effect of these toxins is due to phospholipase A action within the nerve terminal.

摘要
  1. 源自蛇毒的突触前神经毒素β-银环蛇毒素、响尾蛇毒素和太攀蛇毒素,在存在Ca2+和脱氧胆酸盐的情况下,具有与毒性小得多的眼镜蛇磷脂酶A2大致相同的磷脂分解活性。2. Sr2+作为酶的激活剂,其效果远不如Ca2+,对于β-银环蛇毒素和响尾蛇毒素,Sr2+的激活作用仅为3%-6%,对于太攀蛇毒素则为12%。3. 在β-银环蛇毒素和响尾蛇毒素的情况下,Sr2+还会使Ca2+激活的酶抑制80%,但在太攀蛇毒素的情况下仅抑制16%。4. Mg2+对β-银环蛇毒素或响尾蛇毒素没有显著影响,但在存在或不存在Ca2+的情况下都会激活太攀蛇毒素。5. 在不含Ca2+的Sr2+ - Tyrode溶液中,所有这三种毒素在大鼠和小鼠膈膜中均表现出相同的即刻抑制,随后是促进作用,但β-银环蛇毒素和响尾蛇毒素的最终阻断活性仅为3%-10%,太攀蛇毒素为30%。6. 在Sr2+ - Tyrode溶液中,对于任何一种毒素,神经刺激速率的增加对神经肌肉阻滞发展的加速作用都小于在Ca2+ - Tyrode溶液中的情况。7. 从Sr2+ - Tyrode溶液中去除Mg2+不会降低太攀蛇毒素阻断神经肌肉传递的效力,这表明轴膜外表面的酶活性对神经肌肉阻断作用没有贡献。8. 所有结果表明,在轴浆中普遍存在的阳离子环境中,这些毒素的突触前活性与其磷脂分解活性之间存在密切相关性。显然,这些毒素的最终阻断作用是由于神经末梢内的磷脂酶A作用。

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